Swedish Orphan Biovitrum AB (Publ) Form 483 Details
Form 483Source: FDA inspection recordConfirmed against FDA's published inspection data for this establishment and inspection date. FDA has published the inspection and what it cited, but not the form itself, which usually takes six to twelve months.
To check this against FDA, open FDA's record for this establishment on FDA's Data Dashboard, which lists this inspection under FEI 3003455777.
Swedish Orphan Biovitrum AB (Publ)
Stockholm, -, Sweden
Issue DateMay 04, 2018
FEI Number3003455777
CountrySweden
Status
No Warning LetterProduct Type
Drugs